Most of the compounds have physiologically active properties, and their biological properties are often attributed to the heteroatoms contained in their molecules, and most of these heteroatoms also appear in cyclic structures. A Journal, Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999) called Reduction of 3,5-disubstituted pyridines to dihydropyridines, Author is Booker, Evans; Eisner, Ulli, which mentions a compound: 1195-58-0, SMILESS is N#CC1=CC(C#N)=CN=C1, Molecular C7H3N3, Recommanded Product: Pyridine-3,5-dicarbonitrile.
The pyridines (I, R = Me, Et) underwent reduction with NaBH4 to give mixtures of the corresponding 1,4- II and 1,2-dihydropyridines III, resp. The compositions of the isomer mixtures produced in various solvents were determined Reduction of I by NaBH3CN and by B2H6 gave II and III (R = Me, Et), resp.
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